Japan Geoscience Union Meeting 2014

Presentation information

International Session (Oral)

Symbol S (Solid Earth Sciences) » S-IT Science of the Earth's Interior & Techtonophysics

[S-IT03_29PM2] Structure and dynamics of Earth and Planetary deep interiors

Tue. Apr 29, 2014 4:15 PM - 6:00 PM 418 (4F)

Convener:*Satoru Tanaka(Institute for Research on Earth Evolution Japan Agency for Marine-Earth Science and Technology), Takashi Yoshino(Institute for Study of the Earth's Interior, Okayama University), Masanori Kameyama(Geodynamics Research Center, Ehime University), Dapeng Zhao(Department of Geophysics, Tohoku University), John Hernlund(ELSI, Tokyo TECH), Chair:John Hernlund(Earth-Life Science Institute, Tokyo Institute of Technology), Kenji Ohta(Department of Earth and Planetary Sciences, Tokyo Institute of Technology)

5:30 PM - 5:45 PM

[SIT03-27] Experimental approach to the core-mantle boundary region of Mercury

Miho OKAMOTO1, *Satoru URAKAWA1 (1.Dept Earth Sci, Okayama Univ)

Keywords:core, CMB, Mercury

MESSENGER mission revealed precise moment of inertia parameters of Mercury and its surface chemistry [1, 2]. These data allow to model the internal structure of Mercury, which has a large liquid core with 〜2000 km radius and a solid outer shell with 〜400 km thickness [3, 4]. As density of solid outer portion is apparently higher than that of the expected mantle silicate, the solid outer layer must include dense materials. Recent models [3, 4] showed that the Mercury's core contains sulfur and silicon as light elements due to high S fugacity and low oxygen fugacity of its interior. Those models presented a solid FeS layer at bottom of solid outer shell of Mercury as a dense layer, which separated from liquid outer core as a FeS-rich liquid due to liquid immiscibility of the Fe-S-Si ternary system. To investigate the FeS-rich layer at the top of Mercury's core, we performed the high-pressure experiments on the Fe-S-Si system using a KAWAI-type multi-anvil apparatus. Pressure is fixed at 5 GPa corresponding to the CMB of Mercury and temperature is 1800 K, which is 200 K above the liquidus of Fe-S-Si system reported by Sanloup and Fei [5]. Fe-S-Si sample was kept for 30 min at this condition, and then it was quenched into room temperature. Oxygen fugacity of run charges was maintained around 3 log unit below IW buffer. Texture and chemistry of recovered samples were examined by electron microprobe.We found two immiscible liquids in one run charge, which consist of Fe,Si-rich metallic liquid and FeS-rich sulfide liquid. Sulfur content of metallic liquid ranges 6 to 9 at%, which is higher by 〜5 at% than those reported by Morard and Katsura [6]. Differences in texture of recovered samples and run duration between this study and Morard and Katsura [6] suggest that the latter experiments were in disequilibrium state. Our data shows the liquid immiscible region has a narrower extent than the previous estimation and the Mercury immiscible Fe-S-Si core must contain at least 6-9 at% sulfur. The quenched FeS-rich liquid phase consists mainly of crystalline FeS (〜90 vol%) and Fe-Si alloy. In the case that FeS-rich liquid contacted with MgO sample container, (Mg0.8Fe0.2)S crystalline phase coexisted with FeS-rich liquid. Mg-sulfide phase could be made by Fe-Mg exchange reaction between MgO and FeS-rich liquid. In the Mercury core, when FeS-rich liquid ascends to add the bottom of the CMB due to its buoyancy, it makes a stable low density layer. Mg-sulfide phase is produced under low oxygen fugacity and high sulfur fugacity at CMB, and then it incorporates into mantle. This is consistent with the results of X-ray fluorescence spectrometry on the Mercury's surface, which indicates the presence of Mg and Ca sulfides [2].References[1] Margot JL et al., J. Geophys. Res., 117, E00L09, 2012.[2] Nittler LR et al., Science, 333, 1847, 2011.[3] Smith DE et al., Science, 336, 214, 2012.[4] Hauck II SA et al., J. Geophys. Res.: Planets, 118, 1204, 2013.[5] Sanloup C and Fei Y, Phys. Earth Planet. Inter., 147, 57, 2004.[6] Morard G and Katsura T, Geochim. Cosmochim. Acta, 74, 3659, 2010.